Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Phoenix PMIC-108 Panels Recalled by Becton Dickinson & Co. Due to An antibiotic susceptibility test kit may produce false...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Becton Dickinson & Co. directly.
Affected Products
BD Phoenix PMIC-108 Panels, Catalog number 448418, labeled in part ***Becton, Dickinson and Company 7 Loveton Circle Sparks, USA. The BD Phoenix" Automated Microbiology system is intended for the rapid identification (ID) and antimicrobial susceptibility testing (AST) of clinically significant bacteria.
Quantity: 12,250 tests
Why Was This Recalled?
An antibiotic susceptibility test kit may produce false intermediate or false resistant results with clinically significant bacteria.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Becton Dickinson & Co.
Becton Dickinson & Co. has 183 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report